BE Leuven Spinazzi M: Difference between revisions
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|institution=KU Leuven Center for Human Genetics | |institution=KU Leuven Center for Human Genetics | ||
Laboratory for the Research on Neurodegenerative Diseases VIB Center for the Biology of Disease Β | Laboratory for the Research on Neurodegenerative Diseases VIB Center for the Biology of Disease | ||
|address=Herestraat 49 bus 602 | |address=Herestraat 49 bus 602 | ||
|area code=3000 | |area code=3000 | ||
|city=Leuven | |city=Leuven | ||
|country=Belgium | |country=Belgium | ||
|Contact=Spinazzi Marco | |Contact=Spinazzi Marco | ||
|Status=O2k 2015- | |Status=O2k 2015-2018 | ||
|info=[[IOC116]], [[IOC100]] | |||
}} | }} | ||
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== Visiting scientist in the Oroboros O2k-Laboratory == | |||
:::: [[Image:O2k-Network.png|left|40px|link=O2k-Network|O2k-Network]] | |||
[[Spinazzi Marco| Marco Spinazzo]]: Visiting scientist at the [[Oroboros Laboratories: visiting scientists|Oroboros O2k-Laboratory]] from October 21 to October 22 2015. |
Latest revision as of 11:21, 19 November 2019
BE Leuven Spinazzi M
O2k-Network Lab | KU Leuven Center for Human Genetics
Laboratory for the Research on Neurodegenerative Diseases VIB Center for the Biology of Disease |
---|---|
Address | Herestraat 49 bus 602, 3000 |
City | Leuven |
State/Prov | |
Country | Belgium |
Weblink | |
Contact | Spinazzi Marco |
Team | |
Team previous | |
Status | O2k 2015-2018 |
Oroboros Events | IOC116, IOC100 |
Topics |
O2k-Publications
Published | Reference | |
---|---|---|
Cornelissen 2020 Hum Mol Genet | 2020 | Cornelissen T, Spinazzi M, Martin S, Imberechts D, Vangheluwe P, Bird M, De Strooper B, Vandenberghe W (2020) CHCHD2 harboring the Parkinson's disease-linked T61I mutation precipitates inside mitochondria and induces precipitation of wild-type CHCHD2. Hum Mol Genet 29:1096-106. |
Spinazzi 2019 Proc Natl Acad Sci U S A | 2019 | Spinazzi M, Radaelli E, HorrΓ© K, Arranz AM, Gounko NV, Agostinis P, Maia TM, Impens F, Morais VA, Lopez-Lluch G, Serneels L, Navas P, De Strooper B (2019) PARL deficiency in mouse causes Complex III defects, coenzyme Q depletion, and Leigh-like syndrome. Proc Natl Acad Sci U S A 116:277-86. 10.1073/pnas.1811938116 |
Leucci 2016 Nature | 2016 | Leucci E, Vendramin R, Spinazzi M, Laurette P, Fiers M, Wouters J, Radaelli E, Eyckerman S, Leonelli C, Vanderheyden K, Rogiers A, Hermans E, Baatsen P, Aerts S, Amant F, Van Aelst S, van den Oord J, de Strooper B, Davidson I, Lafontaine DL, Gevaert K, Vandesompele J, Mestdagh P, Marine JC (2016) Melanoma addiction to the long non-coding RNA SAMMSON. Nature 531:518-22. |
O2k-Abstracts
update please
Visiting scientist in the Oroboros O2k-Laboratory
Marco Spinazzo: Visiting scientist at the Oroboros O2k-Laboratory from October 21 to October 22 2015.